Benzylamine → HCID 66873152, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:4]([NH:9][C:10]([C:12]2[CH:13]=[C:14]([S:18]([N:21]3[CH2:26][CH2:25][CH2:24][CH:23]([C:27](O)=[O:28])[CH2:22]3)(=[O:20])=[O:19])[CH:15]=[CH:16][CH:17]=2)=[O:11])=[N:5][CH:6]=[CH:7][CH:8]=1.[CH2:30]([NH2:37])[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1>>[CH2:30]([NH:37][C:27]([CH:23]1[CH2:24][CH2:25][CH2:26][N:21]([S:18]([C:14]2[CH:15]=[CH:16][CH:17]=[C:12]([C:10]([NH:9][C:4]3[C:3]([O:2][CH3:1])=[CH:8][CH:7]=[CH:6][N:5]=3)=[O:11])[CH:13]=2)(=[O:19])=[O:20])[CH2:22]1)=[O:28])[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1Participants
3
Procedure
The entitled compound was produced according to the method of Example 57 but using the compound obtained in Example 56 and benzylamine as the starting materials.
Workup
- customThe entitled compound was produced
Sources & evidence
- ORD record
- ord-0416d3a6c1e4482998559b3a11a23970
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08420823B2
Reaction notes
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